Variant report

Variant	nsv899058
Chromosome Location	chr12:48012390-48082482
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:897)
CpG islands
(count:123)
Chromatin interactive
region (count:45)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:897 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:48045429-48047004	HepG2	liver:	n/a	n/a
2	ATF1	chr12:48062471-48062476	K562	blood:	n/a	n/a
3	BACH1	chr12:48030886-48030902	K562	blood:	n/a	n/a
4	BATF	chr12:48066032-48066325	GM12878	blood:	n/a	n/a
5	BHLHE40	chr12:48046326-48046923	HepG2	liver:	n/a	n/a
6	CEBPB	chr12:48061812-48062025	A549	lung:	n/a	n/a
7	CEBPB	chr12:48061853-48061998	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr12:48046644-48046814	HepG2	liver:	n/a	n/a
9	CEBPB	chr12:48061862-48061986	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr12:48046438-48046939	HepG2	liver:	n/a	n/a
11	CEBPB	chr12:48061818-48062042	IMR90	lung:	n/a	n/a
12	CEBPB	chr12:48046536-48046720	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr12:48061848-48061867	HepG2	liver:	n/a	n/a
14	CHD1	chr12:48045392-48045839	IMR90	lung:	n/a	n/a
15	CREB1	chr12:48046460-48047010	HepG2	liver:	n/a	n/a
16	CTCF	chr12:48051485-48051601	GM19240	blood:	n/a	chr12:48051536-48051557 chr12:48051541-48051559
17	CTCF	chr12:48080500-48080650	GM12872	blood:	n/a	n/a
18	CTCF	chr12:48080599-48080656	MCF-7	breast:	n/a	n/a
19	CTCF	chr12:48045391-48045826	GM12878	blood:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
20	CTCF	chr12:48045453-48045740	Medullo	brain:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
21	CTCF	chr12:48045520-48045670	SK-N-SH_RA	brain:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
22	CTCF	chr12:48031100-48031250	HMEC	breast:	n/a	n/a
23	CTCF	chr12:48051420-48051570	HepG2	liver:	n/a	chr12:48051536-48051557 chr12:48051541-48051559
24	CTCF	chr12:48045500-48045650	HRPEpiC	eye:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
25	CTCF	chr12:48045446-48045741	Lung_OC	lung:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
26	CTCF	chr12:48031080-48031230	HAc	cerebellar:	n/a	n/a
27	CTCF	chr12:48051440-48051590	MCF-7	breast:	n/a	chr12:48051536-48051557 chr12:48051541-48051559
28	CTCF	chr12:48080500-48080650	WI-38	lung:	n/a	n/a
29	CTCF	chr12:48045545-48045663	GM13976	blood:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
30	CTCF	chr12:48031080-48031230	HEK293	kidney:	n/a	n/a
31	CTCF	chr12:48017120-48017270	AG09309	skin:	n/a	n/a
32	CTCF	chr12:48045540-48045690	BJ	skin:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
33	CTCF	chr12:48043681-48043749	GM20000	blood:	n/a	n/a
34	CTCF	chr12:48045425-48045790	ECC-1	luminal epithelium:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
35	CTCF	chr12:48045520-48045670	HA-sp	spinal cord:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
36	CTCF	chr12:48051439-48051669	MCF-7	breast:	n/a	chr12:48051536-48051557 chr12:48051541-48051559
37	CTCF	chr12:48051474-48051590	GM19239	blood:	n/a	chr12:48051536-48051557 chr12:48051541-48051559
38	CTCF	chr12:48019129-48019184	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr12:48045540-48045690	AG09319	gingival:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
40	CTCF	chr12:48031060-48031210	Caco-2	colon:	n/a	n/a
41	CTCF	chr12:48045280-48045430	GM12872	blood:	n/a	n/a
42	CTCF	chr12:48080520-48080670	WI-38	lung:	n/a	n/a
43	CTCF	chr12:48080520-48080670	BJ	skin:	n/a	n/a
44	CTCF	chr12:48044905-48044981	Fibrobl	skin:	n/a	n/a
45	CTCF	chr12:48046480-48046630	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr12:48045480-48045630	GM12866	blood:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
47	CTCF	chr12:48031006-48031246	Fibrobl	skin:	n/a	n/a
48	CTCF	chr12:48045500-48045650	NHDF-neo	bronchial:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
49	CTCF	chr12:48045439-48045745	T-47D	breast:	n/a	chr12:48045595-48045613 chr12:48045597-48045618
50	CTCF	chr12:48080540-48080690	NHDF-neo	bronchial:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:48044905-48044955	HepG2	liver:	n/a
2	chr12:48044905-48044955	HepG2	liver:	n/a
3	chr12:48044905-48044955	T-47D	breast:	n/a
4	chr12:48044905-48044955	SKMC	muscle:	n/a
5	chr12:48058400-48058450	Hela-S3	cervix:	n/a
6	chr12:48058400-48058450	NHBE	bronchial:	n/a
7	chr12:48044905-48044955	HCT-116	colon:	n/a
8	chr12:48044905-48044955	K562	blood:	n/a
9	chr12:48044905-48044955	A549	lung:	n/a
10	chr12:48058400-48058450	ProgFib	skin:	n/a
11	chr12:48044905-48044955	HRCEpiC	kidney:	n/a
12	chr12:48044905-48044955	HUVEC	blood vessel:	n/a
13	chr12:48044905-48044955	HPAEpiC	pulmonary alveolar:	n/a
14	chr12:48044905-48044955	BE2_C	brain:	n/a
15	chr12:48058400-48058450	HUVEC	blood vessel:	n/a
16	chr12:48044905-48044955	HRE	kidney:	n/a
17	chr12:48044905-48044955	HCM	heart:	n/a
18	chr12:48058400-48058450	HCF	heart:	n/a
19	chr12:48044905-48044955	PANC-1	pancreas:	n/a
20	chr12:48058400-48058450	MCF10A-Er-Src	breast:	n/a
21	chr12:48058400-48058450	Caco-2	colon:	n/a
22	chr12:48058400-48058450	NB4	blood:	n/a
23	chr12:48058400-48058450	AG09309	skin:	n/a
24	chr12:48044905-48044955	NHDF-neo	bronchial:	n/a
25	chr12:48044905-48044955	Jurkat	blood:	n/a
26	chr12:48058400-48058450	AG09319	gingival:	n/a
27	chr12:48058400-48058450	CMK	blood:	n/a
28	chr12:48044905-48044955	U87	brain:	n/a
29	chr12:48044905-48044955	NT2-D1	testis:	n/a
30	chr12:48058400-48058450	NH-A	brain:	n/a
31	chr12:48058400-48058450	HEEpiC	esophagus:	n/a
32	chr12:48044905-48044955	NH-A	brain:	n/a
33	chr12:48058400-48058450	SKMC	muscle:	n/a
34	chr12:48044905-48044955	HIPEpiC	eye:	n/a
35	chr12:48044905-48044955	NHBE	bronchial:	n/a
36	chr12:48044905-48044955	HEEpiC	esophagus:	n/a
37	chr12:48044905-48044955	AG04449	skin:	fetal
38	chr12:48058400-48058450	T-47D	breast:	n/a
39	chr12:48058400-48058450	HepG2	liver:	n/a
40	chr12:48058400-48058450	GM12891	blood:	n/a
41	chr12:48044905-48044955	MCF-7	breast:	n/a
42	chr12:48058400-48058450	SAEC	small airway:	n/a
43	chr12:48058400-48058450	GM12878	blood:	n/a
44	chr12:48058400-48058450	AG10803	skin:	n/a
45	chr12:48058400-48058450	BE2_C	brain:	n/a
46	chr12:48044905-48044955	HRPEpiC	eye:	n/a
47	chr12:48044905-48044955	HL-60	blood:	n/a
48	chr12:48058400-48058450	HRPEpiC	eye:	n/a
49	chr12:48044905-48044955	ECC-1	luminal epithelium:	n/a
50	chr12:48058400-48058450	NHDF-neo	bronchial:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:48041265..48043377-chr12:48228501..48230073,2	K562	blood:
2	chr12:48040105..48042458-chr12:48048872..48051635,2	K562	blood:
3	chr12:48082467..48084685-chr12:48086429..48089093,4	K562	blood:
4	chr12:48050085..48052473-chr12:48066731..48069120,2	K562	blood:
5	chr12:48082326..48084499-chr12:48098211..48100235,2	MCF-7	breast:
6	chr12:47426505..47427015-chr12:48080605..48081500,2	K562	blood:
7	chr12:48074943..48076860-chr12:48080990..48083244,2	MCF-7	breast:
8	chr12:48081189..48083010-chr12:48095992..48097912,2	K562	blood:
9	chr12:48010127..48013715-chr12:48014407..48017154,4	K562	blood:
10	chr12:48066566..48068151-chr12:48097964..48100528,2	K562	blood:
11	chr12:48042180..48043761-chr12:48096547..48099075,2	K562	blood:
12	chr12:48079877..48082271-chr12:48092983..48095366,2	K562	blood:
13	chr12:48058363..48062042-chr12:48064816..48068792,4	K562	blood:
14	chr12:48072254..48074944-chr12:48080912..48083619,2	K562	blood:
15	chr12:48044527..48046603-chr12:48048041..48049724,2	K562	blood:
16	chr12:48050085..48052473-chr12:48066731..48069120,2	K562	blood:
17	chr12:48059314..48062042-chr12:48063084..48066316,3	K562	blood:
18	chr12:47940612..47941519-chr12:48080237..48081015,3	K562	blood:
19	chr12:48049652..48051782-chr12:48054886..48057074,2	K562	blood:
20	chr12:48049652..48051782-chr12:48054886..48057074,2	K562	blood:
21	chr12:48051468..48053610-chr12:48056133..48058641,2	K562	blood:
22	chr12:47955362..47958310-chr12:48025284..48027406,2	MCF-7	breast:
23	chr12:48074943..48076860-chr12:48080990..48083244,2	MCF-7	breast:
24	chr12:48072254..48074944-chr12:48080912..48083619,2	K562	blood:
25	chr12:48081310..48083010-chr12:48095296..48097492,2	K562	blood:
26	chr12:48014490..48017395-chr12:48029451..48031685,2	MCF-7	breast:
27	chr12:48044022..48046311-chr12:48051570..48054955,3	K562	blood:
28	chr12:48010127..48013715-chr12:48014407..48017154,4	K562	blood:
29	chr12:48058375..48060319-chr12:48098023..48100043,2	K562	blood:
30	chr12:48044527..48046603-chr12:48048041..48049724,2	K562	blood:
31	chr12:47426174..47426833-chr12:48051074..48051739,2	MCF-7	breast:
32	chr12:48045249..48046046-chr12:48080121..48081065,3	MCF-7	breast:
33	chr12:48059314..48062042-chr12:48063084..48066316,3	K562	blood:
34	chr12:48040105..48042458-chr12:48048872..48051635,2	K562	blood:
35	chr12:48076547..48079289-chr12:48099321..48101078,2	K562	blood:
36	chr12:48079504..48082471-chr12:48085134..48087838,3	K562	blood:
37	chr12:47940639..47941454-chr12:48051090..48052018,3	MCF-7	breast:
38	chr12:48014490..48017395-chr12:48029451..48031685,2	MCF-7	breast:
39	chr12:48045249..48046046-chr12:48080121..48081065,3	MCF-7	breast:
40	chr12:48038756..48040401-chr12:48092675..48094968,2	K562	blood:
41	chr12:47801819..47802723-chr12:48080350..48081018,2	MCF-7	breast:
42	chr12:48045147..48046102-chr12:48080596..48081443,2	K562	blood:
43	chr12:48044022..48046311-chr12:48051570..48054955,3	K562	blood:
44	chr12:48064589..48067295-chr12:48089738..48092390,2	K562	blood:
45	chr12:48045147..48046102-chr12:48080596..48081443,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ENDOU-6	chr12:48058373-48058626	NONHSAT027930
2	lnc-ENDOU-6	chr12:48057073-48057373	NONHSAT027930

No data

Variant related genes	Relation type
RPAP3	TF binding region
RPAP3	CpG island
ENSG00000005175	chromatin interactions
ENSG00000257433	chromatin interactions

Extended variants
information (count: 2947 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:2947 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587577	chr12:48012390-48012391	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs150318962	chr12:48012394-48012395	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs10492007	chr12:48012417-48012418	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs534876088	chr12:48012421-48012422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557960511	chr12:48012425-48012426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577904109	chr12:48012432-48012433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537366464	chr12:48012508-48012509	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557297199	chr12:48012510-48012511	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538004228	chr12:48012586-48012587	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573956526	chr12:48012622-48012623	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542752405	chr12:48012706-48012707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs371365846	chr12:48012729-48012730	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543069072	chr12:48012743-48012744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs553182983	chr12:48012746-48012747	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560798320	chr12:48012762-48012763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573421720	chr12:48012792-48012793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541204849	chr12:48012793-48012794	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs137933823	chr12:48012823-48012824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191263716	chr12:48012829-48012830	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543372367	chr12:48012878-48012879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149449448	chr12:48012905-48012906	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528889071	chr12:48012935-48012936	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549001754	chr12:48012974-48012975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565431985	chr12:48012975-48012976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528208970	chr12:48012996-48012997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368402203	chr12:48013033-48013034	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs34473935	chr12:48013047-48013048	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs78585687	chr12:48013062-48013063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374266367	chr12:48013080-48013081	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147222223	chr12:48013144-48013145	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564845290	chr12:48013148-48013149	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557380898	chr12:48013202-48013203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567991153	chr12:48013211-48013212	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112502658	chr12:48013225-48013226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553359858	chr12:48013255-48013256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183458070	chr12:48013267-48013268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556518353	chr12:48013274-48013275	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545533670	chr12:48013313-48013314	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12809264	chr12:48013316-48013317	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs657246	chr12:48013327-48013328	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs374751869	chr12:48013376-48013377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563423485	chr12:48013397-48013398	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs142808609	chr12:48013407-48013408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553841955	chr12:48013435-48013436	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs186679932	chr12:48013500-48013501	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558942301	chr12:48013522-48013523	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs80103036	chr12:48013523-48013524	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551065980	chr12:48013547-48013548	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571467823	chr12:48013566-48013567	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529846302	chr12:48013588-48013589	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Breast cancer	21785460	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1395 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:47998800-48030800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr12:48007200-48024600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:48007400-48012800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr12:48007400-48019800	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr12:48007400-48041800	Weak transcription	HSMMtube	muscle
6	chr12:48007400-48044800	Weak transcription	Aorta	Aorta
7	chr12:48007400-48055400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr12:48007600-48028200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr12:48007600-48032000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr12:48007600-48037600	Weak transcription	Left Ventricle	heart
11	chr12:48008400-48012400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr12:48008400-48014200	Weak transcription	Fetal Muscle Leg	muscle
13	chr12:48008400-48017800	Weak transcription	Lung	lung
14	chr12:48008400-48018200	Weak transcription	Thymus	Thymus
15	chr12:48008400-48019200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr12:48008400-48029000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr12:48008600-48017600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr12:48008600-48018600	Weak transcription	Primary B cells from peripheral blood	blood
19	chr12:48008600-48033400	Weak transcription	Pancreas	Pancrea
20	chr12:48008800-48017800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr12:48009000-48023600	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr12:48009000-48032200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr12:48009200-48018200	Weak transcription	Fetal Intestine Small	intestine
24	chr12:48009400-48014200	Weak transcription	Osteobl	bone
25	chr12:48009600-48012400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr12:48009800-48036200	Weak transcription	Ovary	ovary
27	chr12:48010200-48027800	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr12:48010600-48014000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr12:48011000-48012400	Enhancers	Fetal Stomach	stomach
30	chr12:48011000-48013600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr12:48011200-48013000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr12:48011200-48013400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr12:48011200-48013400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr12:48011200-48013400	Strong transcription	A549	lung
35	chr12:48011200-48017800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr12:48011400-48013200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr12:48011400-48015200	Strong transcription	Primary T cells from cord blood	blood
38	chr12:48011600-48029600	Weak transcription	HSMM	muscle
39	chr12:48011800-48013000	Strong transcription	Primary B cells from cord blood	blood
40	chr12:48012400-48012800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr12:48012400-48013000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr12:48012400-48013400	Weak transcription	Fetal Stomach	stomach
43	chr12:48012800-48014200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr12:48012800-48017800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr12:48012800-48024400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr12:48013000-48016000	Weak transcription	Primary hematopoietic stem cells	blood
47	chr12:48013000-48024400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr12:48013000-48025600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr12:48013000-48029000	Weak transcription	Primary B cells from cord blood	blood
50	chr12:48013200-48024200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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